A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637014



Internal ID6677121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80160974..80169733hg38UCSC Ensembl
Innerchr15:80160974..80169733hg38UCSC Ensembl
Outerchr15:80160715..80169953hg38UCSC Ensembl
chr15:80453316..80462075hg19UCSC Ensembl
Innerchr15:80453316..80462075hg19UCSC Ensembl
Outerchr15:80453057..80462295hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg388760
hg198760
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15305127
SamplesNA18558
Known GenesFAH
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637014
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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